A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4011077



Internal ID11404110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9773959..9774030hg38UCSC Ensembl
chr16:9867816..9867887hg19UCSC Ensembl
chr16:9775317..9775388hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1678363
Supporting Variants
SamplesHuRef
Known GenesGRIN2A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4011077
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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